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Either way, its the start of something big, and Angelo McCaskle is at the helm. The 14-year-old freshman at Thornton Fractional North High School in Calumet City is like most teens his age often found hanging out with friends or helping out at his church. But his spare time also involves doing something many would consider beyond his years running a fashion line. As the founder of his company, ADM fashion, McCaskle spends his days at school and his evenings and weekends creating a vision that will make fashion unique again. Its a slogan McCaskle lives by and meticulously executes in each piece he designs as a way to encourage other teens and adults to embrace their own style. My slogan is so important to me because every teenager and adult wants to copy their style from an idol, he said. I used to be like that, but I felt if my idols can dress and make clothing so unique, I can do the same. As someone who loves design and shopping, McCaskle initially focused on writing a blog about his interests. After consulting his cousin who works in the fashion industry, however, he decided to take it one step further and build a website that would showcase his talents. Eight months later, ADM is growing piece by piece. Because of the companys growth, McCaskle has enlisted the help of two of his friends, freshman India Cooper, who serves as the creative director and website director, and freshman Devin Thomas, who serves as the marketing representative and co-CEO. Currently, the company focuses primarily on producing T-shirts. My goals are to take ADM to the top, said Thomas, who handles the side of the business that involves paperwork, business calls and emails.
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"There were times three and four years ago, before we got the diagnosis, that if I was extra close to my wife, specifically if my face was close to Johanna's face, she would cough," says Scott. I've had to release a lot of what I expected for myself and I've had to accept what has been given to us Scott Watkins But it was only last year that the couple realised they had become unable to physically share their life together. "We had noticed that when Scott would come in [to the room] I would start feeling worse and worse. My normal daily symptoms would just be aggravated," says Johanna. "And then at one point he went to get his haircut and came back in the room and within two minutes I had started my anaphylactic symptoms and he had to leave." A week later Scott tried to see his wife again, but the same thing happened, and they realised their lives would have to change dramatically. "It was this horrible reality that it wasn't going to work," says Johanna. "I was now reacting strongly to my husband. Before this I had reacted to my parents, to many, many other people, but it was horrific when it became Scott." Find out more Image copyright Jen Jacobs Photography (Minneapolis, MN) Listen to Johanna and Scott's interview on Outlook , on the BBC World Service Get the Outlook podcast for more extraordinary real-life stories The treatment and medication that is usually given to MCAS sufferers does not help Johanna, so at the moment the couple do not know when - if ever - their situation will change. "There's not an easy way around this problem. I want to keep Johanna safe and me going to see her compromises her safety," says Scott. "One of the ways I can take care of her now is by not going to see her.